Gene Gene information from NCBI Gene database.
Entrez ID 57336
Gene name Zinc finger protein 287
Gene symbol ZNF287
Synonyms (NCBI Gene)
ZKSCAN13ZSCAN45
Chromosome 17
Chromosome location 17p11.2
Summary This gene encodes a member of the krueppel family of zinc finger proteins, suggesting a role as a transcription factor. Its specific function has not been determined. This gene is located near the Smith-Magenis syndrome region on chromosome 17. [provided
miRNA miRNA information provided by mirtarbase database.
49
miRTarBase ID miRNA Experiments Reference
MIRT1521312 hsa-miR-1184 CLIP-seq
MIRT1521313 hsa-miR-1205 CLIP-seq
MIRT1521314 hsa-miR-1323 CLIP-seq
MIRT1521315 hsa-miR-153 CLIP-seq
MIRT1521316 hsa-miR-1973 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
11
GO ID Ontology Definition Evidence Reference
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IBA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA
GO:0001817 Process Regulation of cytokine production IEA
GO:0003677 Function DNA binding IEA
GO:0005634 Component Nucleus IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9HBT7
Protein name Zinc finger protein 287 (Zinc finger protein with KRAB and SCAN domains 13)
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02023 SCAN 38 127 SCAN domain Domain
PF01352 KRAB 162 203 KRAB box Family
PF00096 zf-C2H2 361 383 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 389 411 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 417 439 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 445 467 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 473 495 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 501 523 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 529 551 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 557 579 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 585 607 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 613 635 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 641 663 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 669 691 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 697 719 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 725 747 Zinc finger, C2H2 type Domain
Sequence
MLASSKRMNSSSRSQILLRWKSDKAQSGPYNVEKEILTSRFLRDTETCRQNFRNFPYPDL
AGPRKALSQLRELCLKWLRPEIHSKEQILELLVLEQFLTILPGEVRTWVKSQYPESSEEA
VTLVEDL
TQILEEEAPQNSTLSQDTPEEDPRGKHAFQTGWLNDLVTKESMTFKDVAVDIT
QEDWELMRPVQKELYKTVTLQNY
WNMVSLGLTVYRPTVIPILEEPWMVIKEILEGPSPEW
ETKAQACTPVEDMSKLTKEETHTIKLEDSYDYDDRLERRGKGGFWKIHTDERGFSLKSVL
SQEYDPTEECLSKYDIYRNNFEKHSNLIVQFDTQLDNKTSVYNEGRATFNHVSYGIVHRK
ILPGEKPYKCNVCGKKFRKYPSLLKHQSTHAKEKSYECEECGKEFRHISSLIAHQRMHTG
EKPYECHQCGKAFSQRAHL
TIHQRIHTGEKPYKCDDCGKDFSQRAHLTIHQRTHTGEKPY
KCLECGKTFSHSSSL
INHQRVHTGEKPYICNECGKTFSQSTHLLQHQKIHTGKKPYKCNE
CWKVFSQSTYL
IRHQRIHSGEKCYKCNECGKAFAHSSTLIQHQTTHTGEKSYICNICGKA
FSQSANL
TQHHRTHTGEKPYKCSVCGKAFSQSVHLTQHQRIHNGEKPFKCNICGKAYRQG
ANL
TQHQRIHTGEKPYKCNECGKAFIYSSSLNQHQRTHTGERPYKCNECDKDFSQRTCLI
QHQRIHTGEKPYACRICGKTFTQSTNLIQHQRVHTGAKHRN
Sequence length 761
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Generic Transcription Pathway
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
PENILE DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Prostate cancer Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
URINARY SYSTEM DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations